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Caption : Accreditation =Accreditation ;

AUSTRIA

OBERÖSTERREICH
LINZ

Accreditation Molecular diagnosis of acute myeloid leukemias (MLL, RUNX1-RUNX1T1, PML-RARalpha, CBFb-MYH11, NPM1, KIT)
Ordensklinikum Linz GmbH Barmherzige Schwestern
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing, PCR based techniques

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GERMANY

Niedersachsen
HANNOVER

Accreditation Diagnosis of acute lymphoblastic leukemia (fusion or rearrangements: AF4-MLL, BCR-ABL, TEL-RUNX1 (TEL-AML1), MLL, E2A-PBX1, MYC-IGH, TCRA/D, IGH, MYC)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : PCR based techniques, FISH

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GERMANY

Niedersachsen
HANNOVER

Accreditation Diagnosis of acute myeloblastic leukemia (fusion genes and rearrangements: RUNX1-RUNX1T1 (AML1-ETO), CBFB-MYH11, PML-RARA, MLLT3-MLL (AF9-MLL), DEK-NUP214 (DEK-CAN), RPN1-EVI1, RBM15-MKL1, MLL, RUNX1-EVI1; aberrations of chromosom 17 (17p13 / TP53), 5/5q, 7/7q; mutation analysis of FLT-TKD, WT1, C- KIT, N- RAS, GATA1, GATA2, RUNX1 (AML1), CEBPA)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of microdeletions/microduplications
Technique(s) : Sanger sequencing, PCR based techniques, FISH

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UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation Molecular diagnosis of Acute Lymphoblastic Leukemia (by detection of fusion transcripts: BCR-ABL and ETV6/RUNX1, RQ-PCR: BCR-ABL and TCRB and TCRG PCR for B and T cell clonality studies)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation Molecular diagnosis of Acute Myeloid Leukaemia (FLT3-itd, NPM1 and cKIT (D816V mutation) genes and by detection of fusion transcripts: BCR/ABL and RUNX1/RUNX1T1, CBFB/MYH11)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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GREECE

ATTIKI
ATHENS

Accreditation Molecular and molecular cytogenetic diagnosis of acute lymphoblastic leukemia (detection by FISH and qRT-PCR of TEL-AML1, BCR-ABL and MLL genes)
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

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GREECE

ATTIKI
ATHENS

Accreditation 'Molecular and molecular cytogenetic diagnosis of acute myeloid leukemia (ETO-AML1 and PML-RARA genes; FLT3, NPM1 and KIT mutation analysis; WT1 overexpression; 17q21, 3q26, 11q23 and 16p13-q22 translocations)'
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Detection of chromosome alterations large in size

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NETHERLANDS

Utrecht
UTRECHT

Accreditation Molecular diagnosis of Familial Platelet Disorder/ Acute Myeloid Leukemia Syndrome (RUNX1 gene)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

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FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation Diagnosis of hereditary thrombocytopenia with normal PMV (RUNX1, ETV6 genes)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
AP-HP.Sorbonne Université - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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NETHERLANDS

Gelderland
NIJMEGEN

Accreditation Molecular diagnosis of Familial Platelet Syndrome with Predisposition to Acute Myelogenous Leukemia (RUNX1 gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

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GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation Diagnosis of acute lymphoblastic leukemia (BCR-ABL1, MLL, MLL-AF4, MLL-ENL, MLL-AF9, ETV6-RUNX1, E2A-PBX)
MVZ Martinsried GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation Diagnosis of acute myeloid leukemia
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics, Immunology
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : Sanger sequencing, PCR based techniques, FISH, Karyotyping

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UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation Molecular diagnosis of Familial platelet disorder with associated myeloid malignancy (RUNX1 gene)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation Diagnosis of acute myeloid leukemia (genes: CBFB-MYH11, RUNX1-RUNX1T1, PML-RARA, FLT3 (ITD, TKD), MLL, MLL-MLLT3, MLL-ELN, MLL-MLLT19, MLL-MLLT4, MLL-ELL, DEK-NUP214, NPM1 (exon 11), CEBP (exon 1), KIT (D816V), WT1 (expression), TET2 (exon 3-11))
MVZ Martinsried GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

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GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation Diagnosis of acute myeloid leukemia
MVZ Martinsried GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : NGS sequencing (except WES), PCR based techniques, FISH, Karyotyping

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GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation Diagnosis of acute lymphoblastic leukemia
MVZ Martinsried GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : NGS sequencing (except WES), PCR based techniques, FISH, Karyotyping

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AUSTRIA

WIEN
WIEN

Accreditation Molecular diagnosis of acute myeloid leukemia (AML1-ETO; CBFB-MYH11; sequencing of CEBPA and NPM1 genes; D816V mutation of the KIT gene; NPM1 quantification)
Medizinische Universität Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing, PCR based techniques

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UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Accreditation Molecular and molecular cytogenetic diagnosis of Acute Myeloid Leukaemia (FLT3, NPM1, RUNX1-RUNX1T1, CBFB-MYH11, PML/RARA and MLL: by PCR, RT-PCR and FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

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UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Accreditation Molecular and molecular cytogenetic diagnosis of Acute Lymphoblastic Leukemia (TAL1, TCF3/PBX1, MLL/AFF1 and TEL/AML1: by PCR, RT-PCR and FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

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UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation Molecular diagnosis of Acute Myeloid Leukaemia - t(8;21)and inv(16) by RT-PCR
Queen Elizabeth University Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation Diagnosis of thrombocytopenia related disorders (gene panel)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing

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GERMANY

Niedersachsen
HANNOVER

Accreditation Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of predisposition to hemopathies (Panel)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

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FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of myelodysplastic syndrome and myelodysplastic acute leukemia (Panel)
GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, PCR based techniques

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of congenital neutropenia (Whole Exome)
AP-HP.Sorbonne Université - Hôpital de la Pitié-Salpêtrière
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques, Whole Exome Sequencing (WES)

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GERMANY

Bayern
MÜNCHEN

Accreditation Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
Pränatal-Medizin München MVZ GmbH
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

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GERMANY

Bayern
MÜNCHEN

Accreditation Diagnosis of acute lymphoblastic leukemia (BCR, CDKN2A, ETV6, FLT3, PDGFRA, PICALM, RUNX1 genes)
Pränatal-Medizin München MVZ GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

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GERMANY

Bayern
MÜNCHEN

Accreditation Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Baden-Württemberg
ULM

Accreditation Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Sachsen
DRESDEN

Accreditation Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Bayern
MÜNCHEN

Accreditation Diagnosis of acute myeloid leukemia with t(8;21)(q22;q22) (CEBPA, FLT3, KIT, RUNX1 genes)
Pränatal-Medizin München MVZ GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
AP-HP.Sorbonne Université - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Bayern
WÜRZBURG

Accreditation Diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universität Würzburg - Biozentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of thrombocytopenia (Panel)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Pre-implantation diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing

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GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation Diagnosis of acute lymphatic leukaemia
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics, Immunology
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : PCR based techniques, FISH, Karyotyping

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NETHERLANDS

Utrecht
UTRECHT

Accreditation Molecular diagnosis of Primary Haemostasis (gene panel; TRO02v17.1)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation Molecular analysis of somatic mutation in tumour tissue for therapeutic decisions (Somatic Tumor Panel, 710 genes)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Mecklenburg-Vorpommern
GREIFSWALD

Accreditation Diagnosis of thrombocytopenias and thrombocytopathies (NGS screening panel, 26 genes)
Institut für Humangenetik der Universitätsmedizin Greifswald
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation Diagnosis of hematopoietic defects (NGS screening panel: 183 genes)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

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BELGIUM

LIEGE
LIEGE

Accreditation Diagnosis of myeloid neoplasms with germline predisposition (gene panel)
CHU de Liège - UniLab Lg
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

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BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Accreditation Diagnosis of neurodevelopmental disorders (gene panel)
Erasme Hospital - ULB
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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BELGIUM

VLAAMS BRABANT
LEUVEN

Accreditation Diagnosis of coagulation disorders (gene panel)
UZ Leuven - Campus Gasthuisberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Accreditation Diagnosis of neurodevelopmental disorders (gene panel)
Universitair Ziekenhuis Brussel
Purpose(s) : Antenatal diagnosis, Pre-implantation diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation Diagnosis of inherited hematologic cancer-predisposing syndrome (Panel)
CLCC Institut Paoli Calmettes
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

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BELGIUM

LIEGE
LIEGE

Accreditation Diagnosis of congenital hematological disorders (gene panel)
CHU de Liège - UniLab Lg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Whole Exome Sequencing (WES)

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GERMANY

Rheinland-Pfalz
MAINZ

Accreditation Diagnosis of acute myeloblastic leukemia with maturation (AML1 and ETO genes)
Zweigpraxis des MVZ der Universitätsmedizin Mainz
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Accreditation Molecular diagnosis of Acute Myeloid Leukaemia (FLT3, NPM, CEBPA, PML-RARa, CBFB-MYH11, RUNX1-RUNX1T1, mutation D816V of c-KIT)
Erasme Hospital - ULB
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

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BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Accreditation Molecular diagnosis of Acute Lymphoblastic Leukaemia (TEL-AML1,E2A-PBX1,BCR-ABL1, WT1)
Erasme Hospital - ULB
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

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CANADA

Ontario
TORONTO

Accreditation Molecular Diagnosis of Acute Myeloid Leukemia (AML/ETO, BCR/ABL, CBFB/MYH11, FLT3/NPM1, PML/RARA, KIT PCR analysis)
Toronto General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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CANADA

Ontario
HAMILTON

Accreditation Molecular Diagnosis of Acute Myeloid Leukemia (AML/ETO, BCR/ABL, CBFB/MYH11, FLT3/NPM1, PML/RARA, RNA analysis)
McMaster University Medical Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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CANADA

Ontario
HAMILTON

Accreditation Molecular Diagnosis of Acute Lymphoid Leukemia (RNA analysis)
McMaster University Medical Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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ITALY

VENETO
VERONA

Molecular diagnosis of myeloid leukemias (BCR, ABL1, JAK2, PML, RARA, AML1 and ETO genes)
Azienda Ospedaliera Universitaria Integrata di Verona - Ospedale Borgo Roma
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of acute myeloid leukemia (FLT3, NPM1 genes and RUNX1/ RUNX1T1, CBFb/MYH11 fusion genes)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES), PCR based techniques

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SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of acute lymphoblastic leukemia (MLL gene and ETV6/ RUNX1 fusion gene)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

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SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
LabGenetics - Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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UNITED KINGDOM

Surrey
SURREY

Molecular diagnosis of Acute Myeloid Leukaemia (PML/RARA, RUNX1T1-RUNX1, inv(16), BCR/ABL and FLT3-ITD/D835 mutations)
Institute of Cancer Research ICR
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

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UNITED KINGDOM

Surrey
SURREY

Molecular diagnosis of Acute Lymphoblastic Leukemia (BCR/ABL, E2A/PBX1, MLL/AF4, TEL/AML1, and SIL/TAL1 (for T-cell leukaemia))
Institute of Cancer Research ICR
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes)
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing

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SPAIN

Comunidad Valenciana
PATERNA

Diagnosis of precursor B-cell acute lymphoblastic leukemia (ABL1, AFF1, BCR, ETV6, KMT2A, PBX1, RUNX1, TCF3 genes)
IMEGEN - Delegación Valencia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

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ITALY

FRIULI VENEZIA GIULIA
UDINE

Molecular diagnosis of myeloid leukemias (PML, RARA, AML1, ETO, CBFB, MYH11, NPM1 genes)
Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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FRANCE

BRETAGNE
RENNES

Diagnosis of acute myeloid leukemia with recurrent genetic anomaly (PML-RARA, NPM1, CBFB-MYH11, RUNX1-RUNX1T1 genes by RT-PCR and RQ-PCR)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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FRANCE

BRETAGNE
RENNES

Diagnosis of precursor B-cell acute lymphoblastic leukemia (BCR-ABL1, RUNX1- ATV6, KMT2A-AFF1, IKZF1 genes by RT-PCR, RQ-PCR, PCR, QPCR, MLPA)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques, MLPA based techniques

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SPAIN

Comunidad Valenciana
ELCHE

Diagnosis of familial platelet syndrome with predisposition to acute myelogenous leukemia (RUNX1 gene)
Bioarray
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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CANADA

Alberta
EDMONTON

Molecular Diagnosis of Familial Acute Myeloid Leukemia - NGS Panel (3 genes)
University of Alberta
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), PCR based techniques, MLPA based techniques, Array based techniques

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AUSTRIA

WIEN
WIEN

Molecular diagnosis of hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome (RUNX1 gene)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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SPAIN

Madrid
MADRID

Diagnosis of hereditary cancer (panel)
Hospital Universitario Fundación Jiménez Díaz
Purpose(s) : Antenatal diagnosis, Pre-implantation diagnosis, Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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SPAIN

La Rioja
LOGROÑO

Diagnosis of hereditary cancer (panel)
Hospital San Pedro
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

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SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of inherited cancer-predisposing syndrome (panel)
Hospital Sant Joan de Déu Barcelona
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

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AUSTRIA

WIEN
WIEN

Diagnosis of acute myeloid leukemia (analysis block: ASXL1, CEBPA, DNMT3A, EZH2, FLT3, IDH1, IDH2, KIT, KRAS, MLL, NPM1, NRAS, PHF6, RUNX1, TET2, TP53, WT1)
Hanusch Krankenhaus
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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SPAIN

Baleares
PALMA DE MALLORCA

Diagnosis of hereditary cancer (panel)
Hospital Universitari Son Espases
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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AUSTRIA

WIEN
WIEN

Diagnosis of myelodysplastic/myeloproliferative diseases (analysis block: ASXL1, CBL, DNMT3A, ETV6, EZH2, IDH1, IDH2, JAK2, KRAS, NRAS, RUNX1, SF3B1, SRSF2, TET2, TP53, U2AF1, ZRSR2 gene)
Hanusch Krankenhaus
Purpose(s) : Somatic genetics, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of solid tumors (panel)
INCLIVA - Facultad de Medicina de la Universidad de Valencia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

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UNITED KINGDOM

Greater Manchester
MANCHESTER

Molecular diagnosis of Acute Myeloid Leukaemia (AML1-MTG8 (ETO) - t(8;21) and CBFB-MYH11 - [inv(16)])
Manchester University NHS Foundation Trust - Manchester Royal Infirmary
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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CZECH REPUBLIC

South Moravia
BRNO

Molecular diagnosis of acute myeloblastic leukemia (AML1/ETO fusion gene)
University hospital Brno
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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FRANCE

NOUVELLE AQUITAINE
PESSAC

Diagnosis of acute lymphoblastic leukemia (detection of MLL-AFF1, TCF3-PBX1, ETV6-RUNX1 and STIL-TAL1 fusion genes)
CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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FRANCE

NOUVELLE AQUITAINE
PESSAC

'Diagnosis of acute lymphoblastic leukemia (detection of CBFB-MYH11, PML-RARA, RUNX1-RUNX1T1 fusion genes; FLT3 and NPM1 gene sequencing)'
CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing, PCR based techniques

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SLOVENIA

SLOVENIA
LJUBLJANA

Molecular and cytogenetic diagnosis of acute lymphoblastic leukemia (TEL/AML1, BCR/ABL, TCF3/PBX1, ETV6/RUNX1gene fusions; FISH and conventional karyotype)
University Medical Center Ljubljana
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size
Technique(s) : Sanger sequencing, Karyotyping

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UNITED KINGDOM

Greater Manchester
MANCHESTER

Molecular diagnosis of Acute Myeloid Leukemia (CBFB-MYH11 [inv(16)], PML-RARA - t(15;17), RUNX1-RUNX1T1 - t(8;21) fusion genes)
Manchester University NHS Foundation Trust - Manchester Royal Infirmary
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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SERBIA

Serbia
BELGRADE

Molecular diagnosis of acute myeloid leukemia (RT-PCR analysis of RUNX1-RUNX1T1, PML-RARA and CBFB-MYH11 fusion genes)
Mother and Child Health Institute of Serbia "Dr Vukan Cupic"
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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SERBIA

Serbia
BELGRADE

Molecular diagnosis of acute lymphoblastic leukemia (RT-PCR analysis of BCR-ABL1, MLL-AFF1, ATV6-AML1 and PBX1-TCF3 fusion genes)
Mother and Child Health Institute of Serbia "Dr Vukan Cupic"
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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SERBIA

Serbia
BELGRADE

'Molecular diagnosis of acute myeloid leukemia with t(8;21) (detection of ETO-AML1 fusion transcript)'
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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SERBIA

Serbia
BELGRADE

'Molecular diagnosis of acute lymphoblastic leukemia (detection of BCR-ABL, MLL-AFF1, TEL-AML1 and E2A-PBX1 fusion transcripts; rearrangements of IGH and CD3G loci)'
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of acute lymphoblastic leukemia (detection of BCR-ABL, MLL-AFF1, TEL-AML1 and E2A-PBX1 fusion transcripts)
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of acute myeloid leukemia (detection of PML-RARA, AML1-ETO, DEK-CAN, CBFB-MYH11 fusion transcripts; NPM1 and FLT3 mutations
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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CANADA

Québec
QUÉBEC

Molecular diagnosis of acute myeloid leukemia (detection of PML-RARa, AML1-ETO, CBFB-MYH11 fusion transcripts; NPM1, CEPBa and FLT3 mutations)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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SPAIN

Galicia
A CORUÑA

Diagnosis of acute myeloid leukemia (CBFB, FLT3, MYH11, PML, RARA, RUNX1, RUNX1T1 genes)
Hospital Universitario da Coruña
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis, Detection of chromosome alterations large in size
Technique(s) : PCR based techniques, FISH, Karyotyping

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SPAIN

Madrid
MADRID

Diagnosis of acute myeloid leukemia with t(8;21)(q22;q22) translocation (RUNX1, RUNX1T1 genes)
Hospital General Universitario Gregorio Marañón
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size
Technique(s) : PCR based techniques, FISH

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FRANCE

HAUTS-DE-FRANCE
LILLE

Diagnosis of tumors of hematopoietic tissues (Panel)
CHU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

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SPAIN

Cataluña
BADALONA

Diagnosis of acute myeloid leukemia with t(8;21)(q22;q22) translocation (RUNX1-RUNX1T1 rearrangement; KIT gene / exons 8 and 17)
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing, PCR based techniques

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SPAIN

Cataluña
BADALONA

Diagnosis of myeloid hemopathy (panel)
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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SPAIN

Madrid
MADRID

Diagnosis of myeloid hemopathy (panel)
Hospital General Universitario Gregorio Marañón
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

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